Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Aavo Valdur Mikelsaar"'
Autor:
Olavi Reinsalu, Ott Scheler, Ruth Mikelsaar, Aavo-Valdur Mikelsaar, Triin Hallap, Ülle Jaakma, Peeter Padrik, Ants Kavak, Andres Salumets, Ants Kurg
Publikováno v:
BMC Veterinary Research, Vol 15, Iss 1, Pp 1-8 (2019)
Abstract Background Usage of sexed semen that allows to choose the gender of the calves, is commonly practiced in livestock industry as a profitable breeding alternative, especially in dairy farming. The flow cytometric cell sorting is the only comme
Externí odkaz:
https://doaj.org/article/eec4b90aeac14b68a3c2854e800cbfed
Autor:
Gerly Sillaste, Tanel Tenson, Agne Velthut-Meikas, Andres Salumets, Sulev Kõks, Peeter Padrik, Aavo-Valdur Mikelsaar, Sergo Kasvandik, Ülle Jaakma, T. Hallap
Publikováno v:
PROTEOMICS
A significant proportion of mammalian fertilization is mediated through the proteomic composition of the sperm surface. These protein constituents can present as biomarkers to control and regulate breeding of agricultural animals. Previous studies ha
Autor:
Ingrid Kalev, Erkki Juronen, Alar Sünter, Andres Piirsoo, Aavo-Valdur Mikelsaar, Peeter Toomik, Ruth Mikelsaar, Anu Kõiveer, Kalmer Karpson
Publikováno v:
Hybridoma. 29:391-401
We report the development of a new mouse anti-titin monoclonal antibody, named MAb Tit1 5H1.1, using the synthetic peptide corresponding to an amino acid sequence in the A-band of the titin molecule as immunogen. In the human skeletal muscle, MAb Tit
Autor:
Mihkel Zilmer, Tarvo Rajasalu, Kersti Oselin, Aavo Valdur Mikelsaar, Piret Pärlist, Toomas Podar, Ingrid Kalev
Publikováno v:
Journal of Diabetes and its Complications. 17:387-391
The purpose of this study was to determine the CCR5-del32 allele frequency in type I (insulin-dependent) and type II (noninsulin-dependent) diabetes patients, and to test whether and how this mutation is associated with both types of diabetes. Thirty
Publikováno v:
Journal of genetics. 93(1)
Autor:
Gunhild Beckman, Astrida Krumina, Chris Tyler-Smith, Lars Beckman, Tatiana Zerjal, Vaidutis Kučinskas, Aavo-Valdur Mikelsaar, Matthew E. Hurles
Publikováno v:
Molecular Biology and Evolution. 18:1077-1087
We analyzed 10 Y-chromosomal binary markers in 363 males from 8 populations in Northern Europe and 5 Y microsatellites in 346 of these individuals. These populations can be grouped according to cultural, linguistic, or geographical criteria, and the
Publikováno v:
European Journal of Epidemiology. 17:213-216
Four hundred and forty two adult individuals of Estonian nationality were examined in different regions of Estonia for the C282Y and H63D HFE mutations to determine the allele and genotype frequencies. The sample consisted only of those people whose
Autor:
Gillian Cooper, Juliette Saillard, João Lavinha, Maria João Prata, Philippos C. Patsalis, Helena B.S.M. Côrte-Real, Peter de Knijff, Astrida Krumina, R. John Mitchell, Siiri Rootsi, William Amos, Yuri E. Dubrova, Mark A. Jobling, Maarja Adojaan, Lars Beckman, Aavo-Valdur Mikelsaar, Ken McElreavey, Anna Jeziorowska, Mukaddes Gölge, Arpita Pandya, Tatiana Zerjal, Syrrou Maria, Gheorghe Stefanescu, Fabrício R. Santos, Dragan Alavantić, Emmeline W. Hill, Anja Gilissen, Richard Villems, Manfred Kayser, Bryan Sykes, Luísa Pereira, Guido Barbujani, David C. Rubinsztein, Gunhild Beckman, Thomas Meitinger, Ronny Decorte, Khedoudja Nafa, S. A. Kravchenko, Aslıhan Tolun, Jüri Parik, Patrizia Malaspina, Elena Bosch, Jayne Nicholson, Zoë H. Rosser, Gaute Brede, Oleg Evgrafov, Carlo Previderè, Gerli Pielberg, Vaidutis Kučinskas, Chris Tyler-Smith, Toomas Kivisild, Manuel Armenteros, Lutz Roewer, António Amorim, Daniel G. Bradley, Matthew E. Hurles, Sanja Glisic, Jaume Bertranpetit, Borut Peterlin, L. A. Livshits, Søren Nørby, Luba Kalaydjieva, Eduardo Arroyo
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
American Journal of Human Genetics
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
American Journal of Human Genetics
Clinal patterns of autosomal genetic diversity within Europe have been interpreted in previous studies in terms of a Neolithic demic diffusion model for the spread of agriculture; in contrast, studies using mtDNA have traced many founding lineages to
Autor:
Aavo-Valdur Mikelsaar, L. I. I. Parts, Erkki Juronen, Siiri Veromann, Aleksei Panov, Leili Soovere, Gunnar Tasa, Riina Pulges, Anne Tiidla, Külle Koka
Publikováno v:
Experimental Eye Research. 71:447-452
Primary open-angle glaucoma, the most common form of glaucoma is a slowly progressive atrophy of the optic nerve, characterized by loss of peripheral visual function and is usually associated with elevated intraocular pressure. The etiology and genet
Publikováno v:
Hybridoma. 15:77-82
The recently discovered human class theta glutathione S-transferase T1-1 (GSTT1-1) is responsible for the GSH-dependent detoxification of naturally occurring monohalomethanes. The detoxifying role of GSTT1-1 has not been investigated in cancer suscep